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Cigdem Altay

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Turkey

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M Sinan Beksac; Fatma Gumruk; Aytemiz Gurgey; Nur Cakar; Sezcan Mumusoglu; Ozgur Ozyuncu; Cigdem Altay
Prenatal diagnosis of hemoglobinopathies in Hacettepe University, Turkey.
Orhan Onalan; Gunay Balta; Ali Oto; Giray Kabakci; Lale Tokgozoglu; Kudret Aytemir; Cigdem Altay; Aytemiz Gurgey; Nasih Nazli
Plasminogen activator inhibitor-1 4G4G genotype is associated with myocardial infarction but not with stable coronary artery disease.
Betul Tavil; Hatice Serapl Kalkanoglu Sivri; Turgay Coskun; Aytemiz Gurgey; Emel Ozyurek; Ali Dursun; Aysegul Tokatli; Cigdem Altay; Fatma Gumruk
Haematological findings in children with inborn errors of metabolism.

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All Publications

2011: M Sinan Beksac; Fatma Gumruk; Aytemiz Gurgey; Nur Cakar; Sezcan Mumusoglu; Ozgur Ozyuncu; Cigdem Altay
Prenatal diagnosis of hemoglobinopathies in Hacettepe University, Turkey.
Pediatric hematology and oncology 2011;28(1):51-5.
2008: Orhan Onalan; Gunay Balta; Ali Oto; Giray Kabakci; Lale Tokgozoglu; Kudret Aytemir; Cigdem Altay; Aytemiz Gurgey; Nasih Nazli
Plasminogen activator inhibitor-1 4G4G genotype is associated with myocardial infarction but not with stable coronary artery disease.
Journal of thrombosis and thrombolysis 2008;26(3):211-7.
2006: Betul Tavil; Hatice Serapl Kalkanoglu Sivri; Turgay Coskun; Aytemiz Gurgey; Emel Ozyurek; Ali Dursun; Aysegul Tokatli; Cigdem Altay; Fatma Gumruk
Haematological findings in children with inborn errors of metabolism.
Journal of inherited metabolic disease 2006;29(5):607-11.
2005: Aytemiz Gürgey; Selin Aytac; Güler Kanra; Gulten Secmeer; Mehmet Ceyhan; Cigdem Altay
Outcome in children with purpura fulminans: report on 16 patients.
American journal of hematology 2005;80(1):20-5.
2005: Lale Olcay; Esra Erdemli; Mehmet Kesimer; Yahya Büyükasik; Hamza Okur; H S Kalkanoğlu; T Coskun; Cigdem Altay
High cystine in platelets from patients with nephropathic cystinosis: a chemical, ultrastructural, and functional evaluation.
Journal of clinical pathology 2005;58(9):939-45.
2005: Stephan M Tanner; Zhongyuan Li; James D Perko; Cihan Oner; Mualla Cetin; Cigdem Altay; Zekiye Yurtsever; Karen L David; Laurence Faivre; Essam A Ismail; Ralph Gustaf Grasbeck; Albert de La Chapelle
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(11):4130-3.
2004: Aytemiz Gurgey; Gunay Balta; Fatma Gumruk; Cigdem Altay
Analysis of some clinical and laboratory aspects of adolescent patients with thrombosis.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004;15(8):657-62.
2004: M Mert Sözen; Cagatay Karaaslan; Reyhan Oner; Fatma Gümrük; M A Ozdemir; Cigdem Altay; Aytemiz Gürgey; Cihan Oner
Severe hemolytic anemia associated with Hb Volga [beta27(B9)Ala-->Asp]: GCC-->GAC at codon 27 in a Turkish family.
American journal of hematology 2004;76(4):378-82.
2004: Sule Unal; Gunay Balta; Feride Duru; Fatma Gumruk; Cigdem Altay; Aytemiz Gurgey
Clinical and laboratory evaluation of Turkish children with thrombosis for homozygous factor V G1691A mutation.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004;15(4):343-6.
2003: Gunay Balta; Fatma Gumruk; Nurten Akarsu; Aytemiz Gurgey; Cigdem Altay
Molecular characterization of Turkish patients with pyrimidine 5' nucleotidase-I deficiency.
Blood 2003;102(5):1900-3.
2003: Gunay Balta; Nazmiye Yuksek; Emel Ozyurek; Ulya Ertem; Gonul Hicsonmez; Cigdem Altay; Aytemiz Gurgey
Characterization of MTHFR, GSTM1, GSTT1, GSTP1, and CYP1A1 genotypes in childhood acute leukemia.
American journal of hematology 2003;73(3):154-60.
2003: Esra Birben; Cihan Oner; Reyhan Oner; Cigdem Altay; Aytemiz Gürgey
Identification of an inframe deletion and a missense mutation in the factor XIIIA gene in two Turkish patients.
European journal of haematology 2003;71(1):39-43.
2003: Gunay Balta; Cigdem Altay; Aytemiz Gurgey
Prevalence of PAI-1 gene 4G/5G genotype in Azerbaijan and Kyrgyzstan populations: literature review.
Journal of thrombosis and haemostasis : JTH 2003;1(4):858-9.
2003: Deniz Aslan; Cigdem Altay
Incidence of high erythrocyte count in infants and young children with iron deficiency anemia: re-evaluation of an old parameter.
Journal of pediatric hematology/oncology 2003;25(4):303-6.
2002: Deniz Aslan; Fatma Gümrük; Mehmet Alikaşifoğlu; Cigdem Altay
Serum alpha-fetoprotein level in Fanconi's anemia: evaluation of 33 Turkish patients.
American journal of hematology 2002;71(4):275-8.
2002: Gunay Balta; Cigdem Altay; Aytemiz Gurgey
PAI-1 gene 4G/5G genotype: A risk factor for thrombosis in vessels of internal organs.
American journal of hematology 2002;71(2):89-93.
2002: Esra Birben; Reyhan Oner; Cihan Oner; Fatma Gümrük; Cigdem Altay; Aytemiz Gürgey
Mutations in coagulation factor XIII A gene in three Turkish patients: two novel mutations and a known insertion.
British journal of haematology 2002;118(1):278-81.
2002: Deniz Aslan; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Importance of RDW value in differential diagnosis of hypochrome anemias.
American journal of hematology 2002;69(1):31-3.
2002: Reyhan Oner; Ceren Acar; Cihan Oner; Idil Yenicesu; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Chronic hemolytic anemia associated with glucose 6-phosphate dehydrogenase (Guadalajara)1 159 C --> T (387 Arg --> Cys) deficiency associated with Gilbert syndrome in a Turkish patient.
Pediatric hematology and oncology 2002;19(1):39-44.
2001: Esra Birben; Cihan Oner; Reyhan Oner; Hatice Mergen; Akif Yesilipek; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: effects of haplotype on phenotype.
Hemoglobin 2001;25(4):441-5.
2001: Esra Birben; Reyhan Oner; Cihan Oner; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Homozygosity for Hb E-Saskatoon [beta22(B4)Glu-->Lys] in a Turkish patient.
Hemoglobin 2001;25(4):409-15.
2001: Reyhan Oner; Cihan Oner; Esra Birben; M Mert Sözen; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G-->A substitution at +22 relative to the beta-globin cap site.
British journal of haematology 2001;115(1):90-4.
2001: Gunay Balta; Aytemiz Gurgey; D K Kudayarov; B Tunc; Cigdem Altay
Evidence for the existence of the PAF acetylhydrolase mutation (Val279Phe) in non-Japanese populations: a preliminary study in Turkey, Azerbaijan, and Kyrgyzstan.
Thrombosis research 2001;101(4):231-4.
2000: L Faivre; Philippe Guardiola; C Lewis; Inderjeet Dokal; Wolfram Ebell; Adriana Zatterale; Cigdem Altay; Janet Poole; David Stones; Mei Lan Kwee; M van Weel-Sipman; C Havenga; N Morgan; Johan P de Winter; Martin Digweed; Anna Savoia; J Pronk; T J L de Ravel; Stander Jansen; Hans Joenje; Eliane Gluckman; Christopher G Mathew
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.
Blood 2000;96(13):4064-70.
2000: Ilja Demuth; M Wlodarski; Alex J Tipping; Neil V Morgan; Johan P de Winter; M Thiel; S Gräsl; Detlev Schindler; Alan D D'Andrea; Cigdem Altay; H Kayserili; Adriana Zatterale; Jürgen Kunze; Wolfram Ebell; Christopher G Mathew; Hans Joenje; Karl Sperling; Martin Digweed
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.
European journal of human genetics : EJHG 2000;8(11):861-8.
2000: Reyhan Oner; Esra Birben; Ceren Acar; Cihan Oner; Ates Kara; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levels.
Hemoglobin 2000;24(3):195-201.
2000: Aytemiz Gurgey; D K Kudayarov; M Tuncer; Hülya Parlak; Cigdem Altay
The factor V Leiden and prothrombin G20210A mutations in Kirghiz population.
Thrombosis and haemostasis 2000;84(2):356.
2000: J Togrul; R Rustamov; Aytemiz Gurgey; S Altay; Cigdem Altay
Prevalence of the prothrombin gene G20210A mutation in Azerbaijan.
British journal of haematology 2000;108(4):887-8.
2000: Reyhan Oner; Fatma Gümrük; Ceren Acar; Cihan Oner; Aytemiz Gürgey; Cigdem Altay
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey.
Haematologica 2000;85(3):320-1.
2000: Fatma Gümrük; Hatice Mergen; Reyhan Oner; Osman Ozcebe; Nilgün Sayinalp; Cihan Oner; Aytemiz Gürgey; Cigdem Altay
Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish family.
Hemoglobin 2000;24(1):23-9.
1999: Aytemiz Gürgey; Idil Yenicesu; T Kanra; Sinasi Ozsoylu; Cigdem Altay; Gönül Hiçsönmez; Sevgi Yetgin; Murat Tuncer; Fatma Gümrük; Mualla Cetin
Autoimmune hemolytic anemia with warm antibodies in children: retrospective analysis of 51 cases.
The Turkish journal of pediatrics 1999;41(4):467-71.
1999: Ahmet Koç; Reyhan Oner; Cihan Oner; Dilek Aktas; M Mert Sözen; Ergül Tunçbilek; Cigdem Altay
Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient.
Hematology and cell therapy 1999;41(4):187-9.
1999: Ahmet F Oner; Aytemiz Gürgey; Hamza Okur; Serafettin Kirazli; Fatma Gümrük; Cigdem Altay
Changes of hemostatic factors in patients with hemoglobinopathies.
The Turkish journal of pediatrics 1999;41(3):323-7.
1999: Quinten Waisfisz; Kathrin Saar; Neil V Morgan; Cigdem Altay; P A J Leegwater; Johan P de Winter; K Komatsu; G R Evans; Rolf-Dieter Wegner; A Reis; Hans Joenje; Fré Arwert; Christopher G Mathew; Jan C Pronk; Martin Digweed
The Fanconi anemia group E gene, FANCE, maps to chromosome 6p.
American journal of human genetics 1999;64(5):1400-5.
1999: Cigdem Altay; Mualla Cetin
Vitamin B12 absorption test and oral treatment in 14 children with selective vitamin B12 malabsorption.
Pediatric hematology and oncology 1999;16(2):159-63.
1999: Sibel T Kinik; A M Tuncer; Cigdem Altay
Transferrin receptor on peripheral blood lymphocytes in iron deficiency anaemia.
British journal of haematology 1999;104(3):494-8.
1999: M Wijker; Neil V Morgan; Sabine Herterich; Carola G M van Berkel; Alex J Tipping; Hans J Gross; Johan J P Gille; Gerard Pals; Maria Savino; Cigdem Altay; S Mohan; Inderjeet Dokal; J Cavenagh; Judith Marsh; M van Weel; JJ Ortega; D Schuler; E Samochatova; M Karwacki; Albert Bekassy; M Abecasis; Wolfram Ebell; Mei Lan Kwee; T J L de Ravel
Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.
European journal of human genetics : EJHG 1999;7(1):52-9.
1999: O Onur; Aysen Sivri; Fatma Gümrük; Cigdem Altay
Beta thalassaemia: a report of 20 children.
Clinical rheumatology 1999;18(1):42-4.
1999: A Koc; Jan C Pronk; Mehmet Alikasifoglu; H Joenje; Cigdem Altay
Variable pathogenicity of exon 43del (FAA) in four Fanconi anaemia patients within a consanguineous family.
British journal of haematology 1999;104(1):127-30.
1998: Ilhan Tezcan; Murat Tuncer; Duygu Uçkan; Mualla Cetin; M Alikaşifoğlu; F Ersoy; Cigdem Altay
Allogeneic bone marrow transplantation in Fanconi anemia from Turkey: a report of four cases.
Pediatric transplantation 1998;2(3):236-9.
1998: Cigdem Altay; Cihan Oner; Reyhan Oner; Fatma Gümrük; Hatice Mergen; Aytemiz Gürgey
Effect of alpha-gene numbers on the expression of beta-thalassemia intermedia, beta-thalassemia and (delta beta)0-thalassemia traits.
Human heredity 1998;48(3):121-5.
1998: Fatma Gümrük; A Gürgey; Cigdem Altay
A case of hypereosinophilic syndrome associated with factor V Leiden mutation and thrombosis.
British journal of haematology 1998;101(1):208-9.
1998: Cihan Oner; Reyhan Oner; Esra Birben; H Balkan; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
HB H disease with homozygosity for red cell G6PD deficiency in a Turkish female.
Hemoglobin 1998;22(2):157-60.
1997: Mualla Cetin; Aytemiz Gürgey; Fatma Gümrük; Cigdem Altay
Serum erythropoietin in children with iron deficiency anemia.
The Turkish journal of pediatrics 1997;39(4):459-64.
1997: J R Lo Ten Foe; Mei Lan Kwee; Martin A Rooimans; Anneke B Oostra; A J Veerman; M van Weel; R M Pauli; N T Shahidi; Inderjeet Dokal; I Roberts; Cigdem Altay; Eliane Gluckman; Robert Alan Gibson; Christopher G Mathew; Fré Arwert; Hans Joenje
Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.
European journal of human genetics : EJHG 1997;5(3):137-48.
1997: Cigdem Altay; M Alikaşifoglu; A Kara; Ergül Tunçbilek; Namik Ozbek; T M Schroeder-Kurth
Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experience.
Clinical genetics 1997;51(5):296-302.
1997: Cigdem Altay; Mualla Cetin
Oral treatment in selective vitamin B12 malabsorption.
Journal of pediatric hematology/oncology 1997;19(3):245-6.
1997: Cigdem Altay; Cihan Oner; Reyhan Oner; Lütfiye Mesci; H Balkan; Sukru Tuzmen; A N Başak; Fatma Gümrük; Aytemiz Gürgey
Genotype-phenotype analysis in HbS-beta-thalassemia.
Human heredity 1997;47(3):161-4.
1997: Cihan Oner; Reyhan Oner; H Balkan; Aytemiz Gürgey; Atilla Yalçin; Ferit Avcu; Cigdem Altay
Molecular analysis of the Turkish form of deletion-inversion (delta beta)(0) thalassaemia.
British journal of haematology 1997;96(2):229-34.
1997: Cihan Oner; Aytemiz Gürgey; Reyhan Oner; H Balkan; Fatma Gümrük; E Baysal; Cigdem Altay
The molecular basis of Hb H disease in Turkey.
Hemoglobin 1997;21(1):41-51.
1996: NS Smetanina; Cihan Oner; E Baysal; Reyhan Oner; G Bozkurt; Cigdem Altay; Aytemiz Gürgey; Adekunle Adekile; LH Gu; TH Huisman
The relative levels of alpha 2-, alpha 1-, and zeta-mRNA in HB H patients with different deletional and nondeletional alpha-thalassemia determinants.
Biochimica et biophysica acta 1996;1316(3):176-82.
1996: Cigdem Altay; Aytemiz Gürgey; A Nazli Basak; Ghazi Tadmouri; T Schroeder-Kurt
Fanconi aplastic anemia associated with beta-thalassemia trait.
American journal of hematology 1996;52(3):239-40.
1996: Aytemiz Gürgey; S Beksaç; E Gümrük; N Cakar; L Mesçi; S Altay; Cihan Oner; Cigdem Altay
Prenatal diagnosis of hemoglobinopathies in Turkey: Hacettepe experience.
Pediatric hematology and oncology 1996;13(2):163-6.
1996: Reyhan Oner; Cihan Oner; Gülsen Erdem; H Balkan; H Ozdağ; M Erkan; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
A novel (delta beta)(0)-thalassemia due to a approximately 30-kb deletion observed in a Turkish family.
Acta haematologica 1996;96(4):232-6.
1995: Aytemiz Gürgey; Cigdem Altay; LH Gu; J Y Leonova; A Delibalta; Cihan Oner; TH Huisman
Hb Hakkari or alpha 2 beta 2 31(B13)Leu-->Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrow.
Hemoglobin 1995;19(3-4):165-72.
1995: Mualla Cetin; Ates Kara; Aytemiz Gürgey; Fatma Gümrük; Gülersu Irken; Sevgi Yetgin; Cigdem Altay
Congenital hypoplastic anemia in six patients: unusual association of short proximal phalanges with mild anemia.
Pediatric hematology and oncology 1995;12(2):153-8.
1995: Cihan Oner; Reyhan Oner; Aytemiz Gürgey; Cigdem Altay
A new Turkish type of beta-thalassaemia major with homozygosity for two non-consecutive 7.6 kb deletions of the psi beta and beta genes and an intact delta gene.
British journal of haematology 1995;89(2):306-12.
1995: Cigdem Altay; Mualla Cetin; Fatma Gümrük; Gülersu Irken; Sevgi Yetgin; Y Laleli
Familial selective vitamin B12 malabsorption (Imerslund-Gräsbeck syndrome) in a pool of Turkish patients.
Pediatric hematology and oncology 1995;12(1):19-28.
1994: Aytemiz Gürgey; Omer Kalayci; Fatma Gümrük; Mualla Cetin; Cigdem Altay
Convulsion after blood transfusion in four beta-thalassemia intermedia patients.
Pediatric hematology and oncology 1994;11(5):549-52.
1994: Dimitar G Efremov; A J Dimovski; E Baysal; Z Ye; Adekunle Adekile; Maria Letícia Ribeiro; G Schiliro; Cigdem Altay; Aytemiz Gürgey; Georgi D Efremov
Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassaemia due to a homozygosity for the IVS-I-6 (T-->C) mutation.
British journal of haematology 1994;86(4):824-30.
1994: T R Sayli; A N Başak; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Imerslund-Gräsbeck syndrome coexisting with beta-thalassemia trait.
Pediatric hematology and oncology 1994;11(2):223-5.
1994: F Duru; Aytemiz Gürgey; Mualla Cetin; T Kanra; Cigdem Altay
Chronic autoimmune hemolytic anemia in children: a report of four patients.
Journal of medicine 1994;25(3-4):231-40.
1993: M A Cürük; A J Dimovski; E Baysal; LH Gu; Ferdane Kutlar; TP Molchanova; B B Webber; Cigdem Altay; Aytemiz Gürgey; TH Huisman
Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients.
American journal of hematology 1993;44(4):270-5.
1993: Lütfiye Mesci; Aytemiz Gürgey; Cigdem Altay
Recent progress in DNA technology.
The Turkish journal of pediatrics 1993;35(3):239-40.
1993: Aytemiz Gürgey; S Beksaç; Lütfiye Mesci; N Cakar; U Karakaş; Abdullah Kutlar; Cigdem Altay
Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I.
The Turkish journal of pediatrics 1993;35(3):159-62.
1993: Fatma Gümrük; Aytekin Besim; Cigdem Altay
Ghosal haemato-diaphyseal dysplasia: a new disorder.
European journal of pediatrics 1993;152(3):218-21.
1993: S Senaati; Fatma Gumruk; P Delbakhsh; Ferhun Balkanci; Cigdem Altay
Gallbladder pathology in pediatric beta-thalassemic patients. A prospective ultrasonographic study.
Pediatric radiology 1993;23(5):357-9.
1992: F Duru; Aytemiz Gürgey; G Oztürk; S Yörükan; Cigdem Altay
Homozygosity for dominant form of hereditary spherocytosis.
British journal of haematology 1992;82(3):596-600.
1992: Fatma Gümrük; Aytemiz Gürgey; F Duru; Cigdem Altay
Reevaluation of iron absorption and serum ferritin in beta-thalassemia intermedia.
Pediatric hematology and oncology 1992;9(4):359-63.
1992: Cihan Oner; A J Dimovski; N F Olivieri; G Schiliro; J F Codrington; Slaheddine Fattoum; Adekunle Adekile; Reyhan Oner; G T Yüregir; Cigdem Altay
Beta S haplotypes in various world populations.
Human genetics 1992;89(1):99-104.
1992: Cihan Oner; A J Dimovski; Cigdem Altay; Aytemiz Gurgey; Y C Gu; TH Huisman; K D Lanclos
Sequence variations in the 5' hypersensitive site-2 of the locus control region of beta S chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes.
Blood 1992;79(3):813-9.
1992: Aytemiz Gürgey; A Rötig; Fatma Gümrük; P Cemeroğlu; F Sarialioğlu; Cigdem Altay
Pearson's marrow-pancreas syndrome in 2 Turkish children.
Acta haematologica 1992;87(4):206-9.
1992: You-Jun Fei; Reyhan Oner; G Bözkurt; LH Gu; Cigdem Altay; Aytemiz Gurgey; Slaheddine Fattoum; E Baysal; TH Huisman
Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations.
Acta haematologica 1992;88(2-3):82-5.
1991: Ferdane Kutlar; H Moscoso; Charles R Kiefer; F A Garver; S Beksaç; L Onderoglu; Aytemiz Gurgey; Cigdem Altay; TH Huisman
Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetuses.
Journal of chromatography 1991;567(2):359-68.
1991: Cigdem Altay; Aytemiz Gurgey; Reyhan Oner; Abdullah Kutlar; Ferdane Kutlar; TH Huisman
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation site.
Hemoglobin 1991;15(4):327-30.
1991: Reyhan Oner; S Agarwal; A J Dimovski; Georgi D Efremov; G H Petkov; Cigdem Altay; Aytemiz Gurgey; TH Huisman
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia.
Hemoglobin 1991;15(1-2):67-76.
1990: Cihan Oner; Aytemiz Gurgey; Cigdem Altay; Ferdane Kutlar; TH Huisman
Variation in the level of fetal hemoglobin in (delta beta) (0)-thalassemia heterozygotes with different numbers of alpha-globin genes.
American journal of hematology 1990;34(3):230-1.
1990: Cigdem Altay; Aytemiz Gürgey
Beta-thalassemia intermedia in Turkey.
Annals of the New York Academy of Sciences 1990;612():81-9.
1990: Aytemiz Gürgey; Sinasi Ozsoylu; Gönül Hiçsönmez; Gülersu Irken; Cigdem Altay
Acute lymphoblastic leukemia in a child with hemoglobins S and Q-Iran.
The Turkish journal of pediatrics 1990;32(1):39-41.
1990: Reyhan Oner; Cigdem Altay; Aytemiz Gurgey; M Cemalettin Aksoy; Yurdanur Kilinç; T A Stoming; A L Reese; Abdullah Kutlar; Ferdane Kutlar; TH Huisman
Beta-thalassemia in Turkey.
Hemoglobin 1990;14(1):1-13.
1989: S Uysal; Banu Anlar; Cigdem Altay; Serafettin Kirazli
Role of protein C in childhood cerebrovascular occlusive accidents.
European journal of pediatrics 1989;149(3):216-8.
1989: J M Gonzalez-Redondo; T A Stoming; Abdullah Kutlar; Ferdane Kutlar; K D Lanclos; E F Howard; You-Jun Fei; M Cemalettin Aksoy; Cigdem Altay; Aytemiz Gurgey
A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with "silent" beta-thalassemia.
Blood 1989;73(6):1705-11.
1989: Ferdane Kutlar; J M Gonzalez-Redondo; Abdullah Kutlar; Aytemiz Gurgey; Cigdem Altay; Georgi D Efremov; K Kleman; TH Huisman
The levels of zeta, gamma, and delta chains in patients with Hb H disease.
Human genetics 1989;82(2):179-86.
1989: You-Jun Fei; Ferdane Kutlar; H F Harris; M M Wilson; A Milana; P Sciacca; G Schiliro; Bruno Masala; Laura Manca; Cigdem Altay
A search for anomalies in the zeta, alpha, beta, and gamma globin gene arrangements in normal black, Italian, Turkish, and Spanish newborns.
Hemoglobin 1989;13(1):45-65.
1989: Aytemiz Gurgey; Cigdem Altay; M Sinan Beksaç; R Bhattacharya; Ferdane Kutlar; TH Huisman
Hydrops fetalis due to homozygosity for alpha-thalassemia-1, -(alpha)-20.5 kb: the first observation in a Turkish family.
Acta haematologica 1989;81(3):169-71.
1989: Abdullah Kutlar; Ferdane Kutlar; M Cemalettin Aksoy; Aytemiz Gurgey; Cigdem Altay; J B Wilson; J C Diaz-Chico; H Hu; TH Huisman
Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemia.
Hemoglobin 1989;13(1):7-16.
1989: Aytemiz Gurgey; Cigdem Altay; J C Diaz-Chico; Ferdane Kutlar; Abdullah Kutlar; TH Huisman
Molecular heterogeneity of beta-thalassemia intermedia in Turkey.
Acta haematologica 1989;81(1):22-7.
1989: T A Stoming; G S Stoming; K D Lanclos; You-Jun Fei; Cigdem Altay; Ferdane Kutlar; TH Huisman
An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene.
Blood 1989;73(1):329-33.
1988: You-Jun Fei; T A Stoming; Georgi D Efremov; Dimitar G Efremov; R Battacharia; J M Gonzalez-Redondo; Cigdem Altay; Aytemiz Gurgey; TH Huisman
Beta-thalassemia due to a T----A mutation within the ATA box.
Biochemical and biophysical research communications 1988;153(2):741-7.
1988: M Ceyhan; I Ozalp; Cigdem Altay
High levels of lactate, pyruvate, and alanine in anemic children.
Clinical pediatrics 1988;27(4):206-9.
1988: Cigdem Altay; Aytemiz Gurgey; J B Wilson; H Hu; B B Webber; Ferdane Kutlar; TH Huisman
Hb F-Baskent or alpha 2A gamma 128(H6)Ala----Thr.
Hemoglobin 1988;12(1):87-9.
1988: J C Diaz-Chico; K G Yang; T A Stoming; Dimitar G Efremov; Abdullah Kutlar; Ferdane Kutlar; M Cemalettin Aksoy; Cigdem Altay; Aytemiz Gurgey; Y Kilinc
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes.
Blood 1988;71(1):248-51.
1987: Cigdem Altay; Abdullah Kutlar; J B Wilson; B B Webber; TH Huisman
Hb P-Nilotic or alpha 2(beta delta)2 in a Turkish family.
Hemoglobin 1987;11(4):395-9.
1986: M Cemalettin Aksoy; Aytemiz Gurgey; Cigdem Altay; Y Kilinc; K C Carstairs; Abdullah Kutlar; S S Chen; B B Webber; J B Wilson; TH Huisman
Some notes about Hb Q-India and Hb Q-Iran.
Hemoglobin 1986;10(2):215-9.
1985: Yurdanur Kilinç; M Kumi; Aytemiz Gurgey; Cigdem Altay; B B Webber; J B Wilson; Abdullah Kutlar; TH Huisman
Hemoglobin O-Padova or alpha(2)30(B11)Glu----Lys beta 2 observed in members of a Turkish family.
Hemoglobin 1985;9(6):621-5.